ONTOLOGY REPORT - ANNOTATIONS


Term:Brugada syndrome 9
go back to main search page
Accession:DOID:0110226 term browser browse the term
Definition:A Brugada syndrome that has material basis in heterozygous mutation in the KCND3 gene on chromosome 1p13. (DO)
Synonyms:exact_synonym: BRGDA9
 primary_id: OMIM:616399
 alt_id: RDO:9001381
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
Brugada syndrome 9 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kcnd3 potassium voltage-gated channel subfamily D member 3 JBrowse link 2 207,923,775 208,140,727 RGD:7240710
RGD:8554872
G Lama4 laminin subunit alpha 4 JBrowse link 20 44,060,715 44,201,966 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14875
    syndrome 4220
      Brugada syndrome 50
        Brugada syndrome 9 2
Path 2
Term Annotations click to browse term
  disease 14875
    Developmental Diseases 7711
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6750
        genetic disease 5997
          monogenic disease 2855
            autosomal genetic disease 2137
              autosomal dominant disease 1098
                Brugada syndrome 9 2
paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.